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Your search keyword '"Jung Woo Son"' showing total 5 results
Start Over Author "Jung Woo Son" Journal journal of cardiovascular ultrasound
5 results on '"Jung Woo Son"'

1. Early Detection for Right Ventricular Dysfunction in Bronchopulmonary Dysplasia without Pulmonary Hypertension

Author

Jung Woo Son

Subjects
medicine.medical_specialty, business.industry, Early detection, 030204 cardiovascular system & hematology, medicine.disease, Pulmonary hypertension, Right ventricular dysfunction, 03 medical and health sciences, 0302 clinical medicine, Text mining, Bronchopulmonary dysplasia, 030225 pediatrics, Internal medicine, Cardiology, Medicine, Radiology, Nuclear Medicine and imaging, Cardiology and Cardiovascular Medicine, business, Editorial Comment
Published
2016

2. A Case of Kommerell's Diverticulum Initially Detected by Transesophageal Echocardiography

Author

Jang-Won Son, Seung Jun Lee, Jin Ho Kim, Jung Woo Son, Geu Ru Hong, Seung-Hyun Lee, Hancheol Lee, Jeong Hun Kim, and Dong-Jun Lee

Subjects
Aortic dissection, medicine.medical_specialty, Right sided aortic arch, business.industry, Aberrant left subclavian artery, Early detection, Case Report, Right-sided aortic arch, Surgical correction, medicine.disease, Asymptomatic, Surgery, surgical procedures, operative, otorhinolaryngologic diseases, medicine, Kommerell's diverticulum, Radiology, Nuclear Medicine and imaging, medicine.symptom, Transesophageal echocardiography, Cardiology and Cardiovascular Medicine, business, Diverticulum, Congenital disorder
Abstract

Kommerell's diverticulum is a rare congenital disorder characterized by typical right sided aortic arch and aberrant left subclavian artery which are usually detected by accident in asymptomatic patients. However, some of patients complain of severe symptoms caused by compression of the adjacent organs or complicated aortic dissection by the diverticulum. Early detection of the disease can lead to elective surgical correction. In this article, we report a Kommerell's diverticulum case initially detected by transesophageal echocardiography.

Published
2013

3. The Case of Isolated Double Atrial Septum with Persistent Interatrial Space

Author

Namsik Chung, Ah Young Ji, Moo Nyun Jin, Changho Song, Young Ju Kim, Jong-Won Ha, Hyuk Jae Chang, Geu Ru Hong, Jung Woo Son, and In Soo Kim

Subjects
medicine.medical_specialty, Double atrial septum, business.industry, Double layered, Case Report, medicine.disease, Asymptomatic, Interatrial space, Atrial septum, Internal medicine, cardiovascular system, medicine, Cardiology, Radiology, Nuclear Medicine and imaging, cardiovascular diseases, Thrombus, medicine.symptom, Cardiology and Cardiovascular Medicine, business, Stroke
Abstract

Double atrial septum is very rare atrial septal malformation which has double layered atrial septum with persistent interatrial space between the two atria. Clinically, most cases of this anomaly are asymptomatic unless manifest as thromboembolic complications, such as stroke, or transient ischemic attack, that thrombus may be originated from this interatrial space. We report a case of a 69-year-old man who was diagnosed with isolated double atrial septum by transthoracic echocardiography.

Published
2013

4. THE CASE OF ISOLATED DOUBLE ATRIAL SEPTUM WITH PERSISTENT INTERATRIAL SPACE.

Author

IN-SOO KIM, MOO-NYUN JIN, CHANGHO SONG, YOUNG JU KIM, AH-YOUNG JI, JUNG-WOO SON, HYUK-JAE CHANG, GEU-RU HONG, JONG-WON HA, and NAMSIK CHUNG

Subjects
ECHOCARDIOGRAPHY, TRANSIENT ischemic attack, LEFT heart ventricle
Abstract

Double atrial septum is very rare atrial septal malformation which has double layered atrial septum with persistent interatrial space between the two atria. Clinically, most cases of this anomaly are asymptomatic unless manifest as thromboembolic complications, such as stroke, or transient ischemic attack, that thrombus may be originated from this interatrial space. We report a case of a 69-year-old man who was diagnosed with isolated double atrial septum by transthoracic echocardiography. [ABSTRACT FROM AUTHOR]

Published
2013
Full Text
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5. A CASE OF KOMMERELL'S DIVERTICULUM INITIALLY DETECTED BY TRANSESOPHAGEAL ECHOCARDIOGRAPHY.

Author

SEUNG-JUN LEE, SEUNG-HYUN LEE, JIN HO KIM, HANCHEOL LEE, DONG-JUN LEE, JEONG HUN KIM, JUNG-WOO SON, JANG-WON SON, and GEU-RU HONG

Subjects
SUBCLAVIAN artery, AORTA surgery, TRANSESOPHAGEAL echocardiography
Abstract

Kommerell's diverticulum is a rare congenital disorder characterized by typical right sided aortic arch and aberrant left subclavian artery which are usually detected by accident in asymptomatic patients. However, some of patients complain of severe symptoms caused by compression of the adjacent organs or complicated aortic dissection by the diverticulum. Early detection of the disease can lead to elective surgical correction. In this article, we report a Kommerell's diverticulum case initially detected by transesophageal echocardiography. [ABSTRACT FROM AUTHOR]

Published
2013
Full Text
View/download PDF

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